WO2018021243A1 - Matériau fusible destiné à un moulage tridimensionnel - Google Patents

Matériau fusible destiné à un moulage tridimensionnel Download PDF

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Publication number
WO2018021243A1
WO2018021243A1 PCT/JP2017/026700 JP2017026700W WO2018021243A1 WO 2018021243 A1 WO2018021243 A1 WO 2018021243A1 JP 2017026700 W JP2017026700 W JP 2017026700W WO 2018021243 A1 WO2018021243 A1 WO 2018021243A1
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Prior art keywords
group
dimensional object
monomer unit
dimensional
polyamide resin
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PCT/JP2017/026700
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English (en)
Japanese (ja)
Inventor
丈士 平井
吉村 忠徳
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花王株式会社
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Priority claimed from JP2017141095A external-priority patent/JP2018024850A/ja
Application filed by 花王株式会社 filed Critical 花王株式会社
Priority to US16/320,940 priority Critical patent/US20190160732A1/en
Priority to CN201780046726.0A priority patent/CN109476840B/zh
Priority to EP17834249.9A priority patent/EP3492511A4/fr
Publication of WO2018021243A1 publication Critical patent/WO2018021243A1/fr

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y70/00Materials specially adapted for additive manufacturing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C67/00Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y10/00Processes of additive manufacturing
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids

Definitions

  • the present invention relates to a soluble material for three-dimensional modeling used as a support material for supporting a three-dimensional object when a three-dimensional object is manufactured by a 3D printer, particularly a hot melt lamination type 3D printer.
  • the 3D printer is a type of rapid prototyping and is a three-dimensional printer that forms a three-dimensional object based on 3D data such as 3D CAD, 3D CG, and the like.
  • a 3D printer system a hot melt lamination system (hereinafter also referred to as an FDM system), an inkjet ultraviolet curing system, an optical modeling system, a laser sintering system, and the like are known.
  • the FDM method is a modeling method for obtaining a three-dimensional object by heating / melting and extruding and laminating polymer filaments, and unlike other methods, does not use a material reaction.
  • FDM 3D printers are small and inexpensive, and have become popular in recent years as devices with little post-processing.
  • a three-dimensional object is formed by stacking a modeling material constituting the three-dimensional object and a support material for supporting the three-dimensional structure of the modeling material.
  • a method for removing the support material from the three-dimensional object precursor there is a method for removing the support material by immersing the three-dimensional object precursor in a high-temperature strong alkaline aqueous solution using a methacrylic acid copolymer as the support material.
  • This method utilizes the fact that the carboxylic acid in the methacrylic acid copolymer is neutralized by an alkali and dissolved in a strong alkaline aqueous solution.
  • the three-dimensional modeling soluble material of the present invention is a three-dimensional modeling soluble material used as a support material for supporting the three-dimensional object when a three-dimensional object is manufactured by an FDM-type 3D printer
  • the three-dimensional modeling soluble material includes a polyamide resin
  • the polyamide resin includes a hydrophilic monomer unit A having a hydrophilic group, a hydrophobic dicarboxylic acid monomer unit B, and a hydrophobic diamine monomer unit C, and the polyamide
  • the ratio of the hydrophilic monomer unit A to the total of all monomer units in the resin is 2.5 mol% or more and less than 13.5 mol%.
  • the three-dimensional object manufacturing method of the present invention includes a step of obtaining a three-dimensional object precursor including a three-dimensional object and a support material, and a support material for removing the support material by bringing the three-dimensional object precursor into contact with neutral water. It is a manufacturing method of the three-dimensional object by the FDM system which has a removal process, Comprising: The material of the said support material is the said soluble material for three-dimensional modeling.
  • the support material of the present invention is a support material that supports a three-dimensional object when the three-dimensional object is manufactured by an FDM-type 3D printer.
  • the support material includes a polyamide resin, and the polyamide resin is hydrophilic.
  • the hydrophilic monomer unit A having a hydrophobic group, the hydrophobic dicarboxylic acid monomer unit B, and the hydrophobic diamine monomer unit C, and the ratio of the hydrophilic monomer unit A to the total of all monomer units in the polyamide resin is 2 0.5 mol% or more and less than 13.5 mol%.
  • Japanese Patent Publication No. 2002-516346 discloses a method for removing a support material by immersing a three-dimensional object precursor in water using polyvinyl alcohol or the like soluble in water as the support material. ing.
  • the support material for the three-dimensional object precursor can be removed without using a strong alkaline aqueous solution, but polyvinyl alcohol or the like has a high affinity for moisture. Therefore, when a three-dimensional modeling soluble material containing polyvinyl alcohol is exposed to high humidity, it absorbs moisture in the air.
  • a 3D modeling soluble material containing water-containing polyvinyl alcohol, etc. is heated / melted / launched / laminated with an FDM 3D printer, the water will evaporate due to high temperature and foam, thereby improving the accuracy of the 3D object. There were times when it was seriously damaged.
  • the present invention is suitable for the production of a three-dimensional object by the FDM method, has moisture absorption resistance, has a high dissolution rate in neutral water, and can be rapidly produced from a three-dimensional object precursor without using a strong alkaline aqueous solution.
  • a three-dimensional modeling soluble material for a support material that can be removed is provided.
  • the present invention can suppress foaming by suppressing the deterioration of accuracy of a three-dimensional object even if it is used for production of a three-dimensional object by a 3D printer after being exposed to high humidity, and can be dissolved in neutral water.
  • a method for producing a three-dimensional object which has a high speed and can quickly remove a support material from a three-dimensional object precursor without using a strong alkaline aqueous solution.
  • the present invention can suppress foaming by suppressing the deterioration of accuracy of a three-dimensional object even if it is used for production of a three-dimensional object by a 3D printer after being exposed to high humidity, and can be dissolved in neutral water.
  • a support material that has a high speed and can be quickly removed from a three-dimensional object precursor without using a strong alkaline aqueous solution.
  • the three-dimensional modeling soluble material of the present invention is a three-dimensional modeling soluble material used as a support material for supporting the three-dimensional object when a three-dimensional object is manufactured by an FDM-type 3D printer
  • the three-dimensional modeling soluble material includes a polyamide resin
  • the polyamide resin includes a hydrophilic monomer unit A having a hydrophilic group, a hydrophobic dicarboxylic acid monomer unit B, and a hydrophobic diamine monomer unit C, and the polyamide
  • the ratio of the hydrophilic monomer unit A to the total of all monomer units in the resin is 2.5 mol% or more and less than 13.5 mol%.
  • the three-dimensional object manufacturing method of the present invention includes a step of obtaining a three-dimensional object precursor including a three-dimensional object and a support material, and a support material for removing the support material by bringing the three-dimensional object precursor into contact with neutral water. It is a manufacturing method of the three-dimensional object by the FDM system which has a removal process, Comprising: The material of the said support material is the said soluble material for three-dimensional modeling.
  • the support material of the present invention is a support material that supports a three-dimensional object when the three-dimensional object is manufactured by an FDM-type 3D printer.
  • the support material includes a polyamide resin, and the polyamide resin is hydrophilic.
  • the hydrophilic monomer unit A having a hydrophobic group, the hydrophobic dicarboxylic acid monomer unit B, and the hydrophobic diamine monomer unit C, and the ratio of the hydrophilic monomer unit A to the total of all monomer units in the polyamide resin is 2 0.5 mol% or more and less than 13.5 mol%.
  • the present invention it is suitable for production of a three-dimensional object by the FDM method, has moisture absorption resistance, has a high dissolution rate in neutral water, and can be used from a three-dimensional object precursor without using a strong alkaline aqueous solution. It is possible to provide a three-dimensional modeling soluble material for a support material that can be quickly removed.
  • the present invention even if it is used for manufacturing a three-dimensional object by a 3D printer after being exposed to high humidity, it is possible to suppress foaming and suppress a decrease in accuracy of the three-dimensional object, and to neutral water.
  • a method for producing a three-dimensional object capable of rapidly removing the support material from the three-dimensional object precursor without using a strong alkaline aqueous solution.
  • the present invention even if it is used for manufacturing a three-dimensional object by a 3D printer after being exposed to high humidity, it is possible to suppress foaming and suppress a decrease in accuracy of the three-dimensional object, and to neutral water. Thus, it is possible to provide a support material that can be rapidly removed from the three-dimensional object precursor without using a strong alkaline aqueous solution.
  • the soluble material for 3D modeling is a soluble material for 3D modeling used as a support material for supporting the 3D object when a 3D object is manufactured by an FDM 3D printer.
  • the three-dimensional modeling soluble material includes a polyamide resin, and the polyamide resin includes a hydrophilic monomer unit A having a hydrophilic group, a hydrophobic dicarboxylic acid monomer unit B, and a hydrophobic diamine monomer unit C, The ratio of the hydrophilic monomer unit A to the total of all monomer units in the polyamide resin is 2.5 mol% or more and less than 13.5 mol%.
  • the support material made of the soluble material for three-dimensional modeling has moisture absorption resistance and has a high dissolution rate in neutral water, so that it can be quickly developed from a three-dimensional object precursor without using a strong alkaline aqueous solution. Can be removed.
  • the reason why the three-dimensional modeling soluble material has such an effect is not clear, but is considered as follows.
  • the three-dimensional modeling soluble material of the present embodiment has a polyamide resin having a specific amount of the hydrophilic monomer unit A, and thus has high solubility in neutral water. Moreover, since the said polyamide resin has the hydrophobic dicarboxylic acid monomer unit B, its hygroscopic property is low. Since the three-dimensional modeling soluble material of this embodiment has such a polyamide resin, the support material containing the three-dimensional modeling soluble material has moisture absorption resistance and is soluble in neutral water. It is considered that the speed is high and it can be quickly removed from the three-dimensional object precursor without using an alkaline aqueous solution.
  • the polyamide resin has a hydrophilic monomer unit A having a hydrophilic group.
  • the hydrophilic monomer unit A is not particularly limited as long as it is a monomer unit having a hydrophilic group.
  • a monomer for inducing the hydrophilic monomer unit A is also referred to as monomer A.
  • the hydrophilic group includes a primary amino group, a secondary amino group, a tertiary amino group, from the viewpoint of solubility in neutral water and the ease of the polymerization reaction during the production of the polyamide resin.
  • examples thereof include at least one selected from the group consisting of a quaternary ammonium base, an oxyethylene group, a hydroxyl group, a carboxyl group, a carboxyl base, a phosphate group, a phosphate group, a sulfonate group, and a sulfonate group.
  • the secondary amino group is —NHR 1 group (where R 1 is linear or branched, from the viewpoint of solubility in neutral water and ease of polymerization reaction during the production of polyamide resin. At least one selected from the group consisting of a secondary amino group represented by (II) and a secondary amino group represented by —NH— group.
  • the tertiary amino group is a —NR 2 R 3 group (provided that R 2 is linear or branched from the viewpoint of solubility in neutral water and ease of polymerization reaction during the production of polyamide resin.
  • Jo having 1 to 4 carbon indicates an alkyl group
  • R 3 is a tertiary amino group represented by denotes a straight or branched carbon atoms 1 to 14 alkyl group.
  • -NR At least one selected from the group consisting of tertiary amino groups represented by a 4 -group (wherein R 4 represents a linear or branched alkyl group having 1 to 4 carbon atoms) is preferred. .
  • the quaternary ammonium base is —N + ⁇ R 5 R 6 R 7 ⁇ ⁇ X ⁇ (where, from the viewpoint of solubility in neutral water and ease of polymerization reaction during the production of polyamide resin.
  • R 5 , R 6 and R 7 each independently represent a hydrogen atom or an alkyl group having 1 to 14 carbon atoms
  • X ⁇ represents a hydroxy ion, a halogen ion, CH 3 SO 4 — or CH 3 CH 2 SO. 4 - at least one or more preferably selected from the group consisting of quaternary ammonium base represented by the illustrated).
  • the oxyethylene group is — ⁇ CH 2 CH 2 O ⁇ n — (where n represents an average number) from the viewpoint of solubility in neutral water and the ease of polymerization reaction during the production of polyamide resin.
  • R 8 is 4 or more and 50 or less
  • the carboxyl base is —COOM 1 (where M 1 represents a counter ion of the carboxyl group constituting the carboxyl base, from the viewpoint of solubility in neutral water and the ease of the polymerization reaction during the production of the polyamide resin.
  • At least one selected from the group consisting of sodium ions, potassium ions, lithium ions, calcium ions, magnesium ions, ammonium ions, barium ions, and zinc ions is preferable, sodium More preferably, at least one selected from the group consisting of ions, potassium ions, lithium ions, magnesium ions, and ammonium ions, more preferably at least one selected from the group consisting of sodium ions and potassium ions, sodium ions Gayo Further preferred.)
  • Carboxyl base is preferably represented by.
  • the phosphate group is —PO 4 M 2 2 , —PO 4 HM 2 , and —PO 4 M 2 from the viewpoint of solubility in neutral water and the ease of polymerization reaction during the production of polyamide resin.
  • M 2 represents a counter ion of a phosphate group constituting a phosphate group, and from the viewpoint of solubility in neutral water, sodium ion, potassium ion, lithium ion, calcium ion, magnesium ion, ammonium ion, barium.
  • At least one selected from the group consisting of ions and zinc ions more preferably at least one selected from the group consisting of sodium ions, potassium ions, lithium ions, magnesium ions, and ammonium ions, sodium ions, And at least one selected from the group consisting of potassium ions is more preferred.
  • Ku at least one or more preferably sodium ion is selected from the group consisting of phosphoric acid base represented by even more preferred.).
  • the sulfonate group is —SO 3 M 3 (where M 3 is a sulfonic acid constituting the sulfonate group).
  • M 3 is a sulfonic acid constituting the sulfonate group.
  • at least one selected from the group consisting of sodium ions, potassium ions, lithium ions, magnesium ions, and ammonium ions and more preferably at least one selected from the group consisting of sodium ions and potassium ions. More preferably, sodium ions are more Preferred.
  • Sulfonate is preferably represented by.
  • the monomer A is a carboxylic acid from the viewpoint of solubility in neutral water, the viewpoint of moisture absorption resistance, the viewpoint of heat resistance required for modeling by a 3D printer, and the ease of polymerization reaction during the production of polyamide resin.
  • At least one selected from the group consisting of amines and amino acids is preferred, and carboxylic acids are more preferred.
  • carboxylic acids aromatic carboxylic acids are preferable from the same viewpoint, and hydroxy group-containing aromatic dicarboxylic acid, primary amino group-containing aromatic dicarboxylic acid, sulfonic acid group-containing aromatic dicarboxylic acid, and sulfonate group-containing Aromatic dicarboxylic acids are more preferred.
  • 5-hydroxyisophthalic acid, 1,3,5-benzenetricarboxylic acid, 5-aminoisophthalic acid, 5-sulfoisophthalic acid, 2-sulfoterephthalic acid, and 4-sulfo-2,6- At least one selected from the group consisting of naphthalenedicarboxylic acid is preferable, at least one selected from the group consisting of 5-sulfoisophthalic acid and 2-sulfoterephthalic acid is more preferable, and 5-sulfoisophthalic acid is more preferable.
  • the content of the hydrophilic group in the polyamide resin is preferably 0.5 mmol / g or more, more preferably 0.6 mmol / g or more, and 0.7 mmol / g or more. Is more preferable, and from the viewpoint of moisture absorption resistance and from the viewpoint of heat resistance required for modeling by a 3D printer, it is preferably less than 1.0 mmol / g, preferably 0.8 mmol / g or less, and more preferably 0.75 mmol / g or less. preferable.
  • content of a hydrophilic group is measured by the method as described in an Example.
  • the ratio of the substance amount of the hydrophilic monomer unit A to the total substance amount of all the monomer units in the polyamide resin is 2.5 mol% or more from the viewpoint of solubility in neutral water, and 4 mol% or more. Is preferably 6 mol% or more, more preferably 8 mol% or more, still more preferably 10 mol% or more, and from the viewpoint of moisture absorption resistance and the heat resistance required for modeling by a 3D printer, less than 13.5 mol% 11.5 mol% or less is preferable, 10.0 mol% or less is more preferable, and 9.5 mol% or less is still more preferable.
  • the composition of the monomer unit of the polyamide resin is measured by the method described in the examples.
  • the polyamide resin has a hydrophobic dicarboxylic acid monomer unit B.
  • the dicarboxylic acid monomer unit B does not have the hydrophilic group.
  • the dicarboxylic acid for deriving the hydrophobic dicarboxylic acid monomer unit B is also referred to as dicarboxylic acid B.
  • the dicarboxylic acid B is not particularly limited as long as it is a dicarboxylic acid, but from the viewpoint of solubility in neutral water, from the viewpoint of moisture absorption resistance, from the viewpoint of heat resistance required for modeling by a 3D printer, and during polyamide resin production From the viewpoint of ease of polymerization reaction, at least one selected from the group consisting of aromatic dicarboxylic acids, aliphatic dicarboxylic acids, and alicyclic dicarboxylic acids is preferred.
  • the group consisting of terephthalic acid, isophthalic acid, 2,5-furandicarboxylic acid, 2,6-naphthalenedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, and 1,3-adamantanedicarboxylic acid More preferably, at least one selected from the group consisting of terephthalic acid, 2,5-furandicarboxylic acid, and 2,6-naphthalenedicarboxylic acid is more preferable, and terephthalic acid is still more preferable.
  • the ratio of the substance amount of the hydrophobic dicarboxylic acid monomer unit B in the polyamide resin to the total substance amount of all monomer units in the polyamide resin is preferably 10 mol% or more from the viewpoint of moisture absorption resistance, and is 20 mol%.
  • the above is more preferable, 30 mol% or more is further preferable, 35 mol% or more is more preferable, 40 mol% or more is further more preferable, 42 mol% or more is further more preferable, and 47.5 mol from the viewpoint of solubility in neutral water.
  • the ratio of the substance amount of the hydrophobic dicarboxylic acid monomer unit B in the polyamide resin to the total substance amount of all the monomer units in the polyamide resin is determined in terms of moisture absorption resistance and dissolved in neutral water. From the viewpoint of safety, 10 to 47.5 mol% is preferable, 20 to 45 mol% is more preferable, and 30 to 42 mol% is still more preferable.
  • the molar ratio of the hydrophilic monomer unit A to the hydrophobic dicarboxylic acid monomer unit B is determined by solubility in neutral water, moisture absorption resistance, and From the viewpoint of heat resistance required for modeling by a 3D printer, 10/90 or more is preferable, 15/85 or more is more preferable, 18/82 or more is further preferable, 20/80 or more is further more preferable, and the same viewpoint 27 / 73 is preferable, 25/75 or less is more preferable, and 21/79 or less is still more preferable.
  • the polyamide resin has a hydrophobic diamine monomer unit C.
  • the hydrophobic diamine monomer unit C does not have the hydrophilic group.
  • the diamine for deriving the hydrophobic diamine monomer unit C is also referred to as diamine C.
  • the diamine C is not particularly limited, and at least one selected from the group consisting of aliphatic diamines, alicyclic diamines, and aromatic diamines can be used, and the ease of the polymerization reaction during polyamide resin production. In view of the above, an aliphatic diamine is preferable.
  • the number of carbon atoms of the diamine C is from the viewpoint of solubility in neutral water, from the viewpoint of moisture absorption resistance, from the viewpoint of heat resistance required for modeling by a 3D printer, and from the viewpoint of ease of polymerization reaction when producing a polyamide resin. 2 or more, preferably 3 or more, more preferably 4 or more, from the viewpoint of solubility in neutral water, the viewpoint of moisture absorption resistance, and the heat resistance required for modeling by a 3D printer, 20 or less Is preferably 15 or less, more preferably 10 or less.
  • aliphatic diamine examples include ethylene diamine, trimethylene diamine, tetramethylene diamine, pentamethylene diamine, hexamethylene diamine, heptamethylene diamine, octamethylene diamine, nonane diamine, and decane diamine.
  • hexamethylenediamine is preferable from the viewpoints of solubility in neutral water, moisture absorption resistance, and toughness (strength) required for modeling by a 3D printer.
  • alicyclic diamine examples include 4,4'-diamino-3,3'-dimethyldicyclohexylmethane, diaminecyclohexane, and isophoronediamine.
  • diamine cyclohexane and isophorone diamine is preferable from the viewpoint of solubility in neutral water, moisture absorption resistance, and toughness (strength) required for modeling by a 3D printer. More preferred is diamine cyclohexane.
  • aromatic diamine examples include phenylenediamine, diethyltoluenediamine, and 4,4'-diaminodiphenylmethane.
  • phenylenediamine diethyltoluenediamine
  • 4,4'-diaminodiphenylmethane examples include phenylenediamine, diethyltoluenediamine, and 4,4'-diaminodiphenylmethane.
  • at least one or more selected from the group consisting of phenylenediamine and diethyltoluenediamine is preferable from the viewpoints of solubility in neutral water, moisture absorption resistance, and toughness (strength) required for modeling by a 3D printer. More preferred is phenylenediamine.
  • the diamine C is at least selected from the group consisting of hexamethylenediamine, diaminecyclohexane, and phenylenediamine from the viewpoint of solubility in neutral water, moisture absorption resistance, and toughness (strength) required for modeling by a 3D printer.
  • One or more are preferable, at least one selected from the group consisting of hexamethylenediamine and phenylenediamine is more preferable, and hexamethylenediamine is still more preferable.
  • the diamine C is at least one selected from the group consisting of hexamethylene diamine, diamine cyclohexane, and phenylene diamine, hexamethylene diamine, diamine cyclohexane, phenylene with respect to the total amount of all diamine monomer units in the polyamide resin.
  • the total proportion of the diamine substances is preferably 50 mol% or more, more preferably 70 mol% or more, and 80 mol% from the viewpoints of solubility in neutral water, moisture absorption resistance, and heat resistance required for modeling by a 3D printer. % Or more is more preferable, 90 mol% or more is more preferable, substantially 100 mol% is still more preferable, and 100 mol% is still more preferable.
  • substantially 100 mol% means the case where substances other than hexamethylene diamine, diamine cyclohexane, and phenylene diamine are inevitably mixed.
  • the polyamide resin can be exemplified by the following general formulas (1) to (6).
  • p1 and q1 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water. )
  • p2 and q2 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water. )
  • p3 and q3 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water. )
  • p4 and q4 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water. )
  • p5 and q5 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water. )
  • p6 and q6 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water. )
  • the weight average molecular weight of the polyamide resin is preferably 3000 or more, more preferably 3500 or more, still more preferably 4000 or more, and solubility in neutral water, from the viewpoint of improving toughness required for a three-dimensional modeling soluble material. And 70000 or less, more preferably 50000 or less, still more preferably 30000 or less, and even more preferably 20000 or less, from the viewpoint of formability by a 3D printer.
  • a weight average molecular weight is measured by the method as described in an Example.
  • the glass transition temperature of the polyamide resin is preferably 50 ° C. or higher, more preferably 60 ° C. or higher, still more preferably 70 ° C. or higher, still more preferably 80 ° C. or higher, from the same viewpoint, from the viewpoint of formability by a 3D printer. 250 ° C. or lower is preferable, and 220 ° C. or lower is more preferable.
  • a glass transition temperature is measured by the method as described in an Example.
  • the polyamide resin may have a monomer unit other than the monomer unit A, the dicarboxylic acid monomer unit B, and the diamine monomer unit C as long as the effects of the present embodiment are not impaired.
  • the method for producing the polyamide resin is not particularly limited, and a conventionally known method for producing a polyamide resin can be applied.
  • the content of the polyamide resin in the soluble material for three-dimensional modeling can be adjusted within a range that does not impair the effect of the present embodiment, but it is soluble in neutral water, moisture absorption resistance, and depending on the 3D printer. From the viewpoint of heat resistance required for modeling, it is preferably 30% by mass or more, more preferably 50% by mass or more, still more preferably 60% by mass or more, still more preferably 70% by mass or more, and even more preferably 80% by mass or more. 90 mass% or more is still more preferable, 95 mass% or more is further more preferable, substantially 100 mass% is still more preferable, and 100 mass% is still more preferable. In addition, substantially 100 mol% means that a substance other than the polyamide resin is inevitably mixed.
  • the glass transition temperature of the soluble material for three-dimensional modeling is preferably 50 ° C. or higher, more preferably 60 ° C. or higher, still more preferably 70 ° C. or higher, and still more preferably 80 ° C. or higher, from the viewpoint of formability by a 3D printer. From the same viewpoint, 250 ° C. or lower is preferable, and 220 ° C. or lower is more preferable.
  • the shape of the soluble material for three-dimensional modeling is not particularly limited, and examples thereof include a pellet shape, a powder shape, and a filament shape, but a filament shape is preferable from the viewpoint of modeling by a 3D printer.
  • the diameter of the filament is preferably 0.5 mm or more, more preferably 1.0 mm or more, and preferably 3.0 mm or less from the same viewpoint, from the viewpoints of formability by a 3D printer and improvement of accuracy of a three-dimensional object. 0 mm or less is more preferable, and 1.8 mm or less is still more preferable.
  • the draw ratio in the drawing process is preferably 1.5 times or more, more preferably 2 times or more, more preferably 3 times or more, still more preferably 5 times or more, and the same viewpoint from the viewpoint of both toughness improvement and water solubility.
  • stretching process has the preferable inside of the range of the temperature 110 degreeC higher than the said glass transition temperature from the temperature 20 degreeC lower than the glass transition temperature of the said soluble material for three-dimensional modeling.
  • the lower limit of the stretching temperature is preferably 10 ° C. lower than the glass transition temperature from the viewpoint of toughness improvement and thermal stability, and more preferably the same temperature as the glass transition temperature.
  • the upper limit of the stretching temperature is more preferably 110 ° C. higher than the glass transition temperature, more preferably 100 ° C.
  • the stretching may be performed while air cooling when the resin is discharged from the extruder, or may be heated by hot air or a laser. Moreover, the said extending
  • the three-dimensional modeling soluble material may contain a polymer other than the polyamide resin for the purpose of improving the physical properties of the three-dimensional modeling soluble material as long as the effects of the present embodiment are not impaired.
  • polymers include water-soluble polymers such as polyvinyl alcohol, polyethylene glycol, poly (ethylene glycol / propylene glycol), carboxymethylcellulose, and starch; hydrophobic polymers such as polymethyl methacrylate; hard segments and soft Segmented polyether ester, polyether ester amide, polyurethane and other elastomers, block copolymers of ionic monomers and water-soluble nonionic monomers and hydrophobic monomers, styrene-butadiene, alkyl methacrylates (1-18 carbon atoms) ) -A thermoplastic elastomer composed of alkyl acrylate (having 1 to 18 carbon atoms); a graft polymer obtained by grafting a polymer such as polyacrylic acid or N, N-dimethylacryl
  • the three-dimensional modeling soluble material contains a polymer other than the polyamide resin
  • the affinity and compatibility between the polymer and the polyamide resin are increased to improve the performance of the three-dimensional modeling soluble material and the three-dimensional modeling solubility.
  • the three-dimensional modeling soluble material can contain a compatibilizing agent.
  • the compatibilizer include (i) a monomer having a glycidyl group, an isocyanate group, an epoxy group, an oxazoline group, and / or a monomer having an acid anhydride structure such as maleic anhydride, and acrylic acid or alkyl methacrylate.
  • a copolymer with ethylene, propylene, vinyl acetate, etc. (ii) a block copolymer comprising two or more of the polymers shown below; polyester, polyamide, and acrylic acid, methacrylic acid, acrylic acid or alkyl methacrylate A polymer / copolymer comprising at least one monomer selected from acrylamide, N, N-dimethylacrylamide, ethylene, propylene, butadiene, isopropylene, vinyl acetate, ethylene glycol, or propylene glycol, and (iii) A group consisting of two or more of the indicated polymers Raft copolymer; polyester, polyamide, acrylic acid, methacrylic acid, acrylic acid or alkyl methacrylate, acrylamide, N, N-dimethylacrylamide, ethylene, propylene, butadiene, isopropylene, vinyl acetate, ethylene glycol, or propylene And a polymer / copolymer comprising at least one monomer selected from glyco
  • the soluble material for three-dimensional modeling may contain other components as long as the effects of the present embodiment are not impaired.
  • the other components include polyamide resins other than the above polyamide resins, polymers other than polyamide resins, plasticizers such as polyalkylene glycol diesters of benzoic acid, calcium carbonate, magnesium carbonate, glass balls, graphite, carbon black, carbon Examples thereof include fillers such as fiber, glass fiber, talc, wollastonite, mica, alumina, silica, kaolin, whisker, and silicon carbide.
  • the method for producing a three-dimensional object includes a step of obtaining a three-dimensional object precursor including a three-dimensional object and a support material, and a support for removing the support material by bringing the three-dimensional object precursor into contact with neutral water. It is a manufacturing method of the three-dimensional object by the hot melt lamination system which has a material removal process, Comprising: The material of the said support material is the said soluble material for three-dimensional modeling.
  • foaming can be suppressed even when used for manufacturing a three-dimensional object by a 3D printer after being exposed to high humidity, and a decrease in accuracy of the three-dimensional object can be suppressed.
  • the support material can be quickly removed from the three-dimensional object precursor without using a strong alkaline aqueous solution because of its high dissolution rate in neutral water. The reason why the manufacturing method of the three-dimensional object has such an effect is not clear, but the same reason as the reason why the soluble material for three-dimensional modeling has the effect can be considered.
  • Step of obtaining a three-dimensional object precursor including a three-dimensional object and a support material The step of obtaining a three-dimensional object precursor including a three-dimensional object and a support material is performed in a three-dimensional manner using a known hot-melt lamination type 3D printer except that the material of the support material is the soluble material for three-dimensional modeling.
  • a step of obtaining a three-dimensional object precursor including a three-dimensional object and a support material in the object manufacturing method can be used.
  • the modeling material that is the material of the three-dimensional object can be used without particular limitation as long as it is a resin that is used as a modeling material in a conventional FDM three-dimensional object manufacturing method.
  • the molding material includes ABS resin, polylactic acid resin, polycarbonate resin, 12-nylon, 6,6-nylon, 6-nylon, polyphenylsulfone resin, polyetheretherketone, and polyetherimide.
  • ABS resin and / or polylactic acid resin are more preferable, and ABS resin is more preferable from the viewpoint of the formability by a 3D printer.
  • the support material removing step the support material is removed by bringing the three-dimensional object precursor into contact with neutral water.
  • the method of bringing the three-dimensional object precursor into contact with neutral water is preferably a method of immersing the three-dimensional object precursor in neutral water from the viewpoint of cost and ease of work. From the viewpoint of improving the removability of the support material, it is possible to promote the dissolution of the support material by irradiating ultrasonic waves during the immersion.
  • the neutral water examples include ion-exchanged water, pure water, tap water, and industrial water, but ion-exchanged water and tap water are preferable from the viewpoint of economy.
  • the neutral water may contain the water-soluble organic solvent in the range which does not damage the shaped three-dimensional object.
  • water-soluble organic solvents include lower alcohols such as methanol, ethanol and 2-propanol, glycol ethers such as propylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monotertiary butyl ether and diethylene glycol monobutyl ether, acetone and methyl ethyl ketone. And ketones.
  • the content of the water-soluble organic solvent in the neutral water is preferably 0.1% by mass or more from the viewpoint of solubility and damage to the shaped three-dimensional object, 0.5% by mass or more is more preferable, 1% by mass or more is further preferable, 3% by mass or more is further preferable, 50% by mass or less is preferable, 40% by mass or less is more preferable, and 30% by mass or less is more preferable. 20% by mass or less is even more preferable.
  • the amount of the neutral water used is preferably 10 times by mass or more, more preferably 20 times by mass or more with respect to the support material from the viewpoint of solubility of the support material, and 10,000 from the support material from the viewpoint of economy.
  • the mass times or less are preferable, the 5000 mass times or less are more preferable, the 1000 mass times or less are more preferable, and the 100 mass times or less are more preferable.
  • the time for bringing the soluble material for 3D modeling into contact with neutral water is preferably 5 minutes or more from the viewpoint of the removability of the support material, and reducing damage to the 3D object by contacting with neutral water for a long time. From the viewpoint of viewpoint and economy, it is preferably 180 minutes or shorter, more preferably 120 minutes or shorter, and even more preferably 90 minutes or shorter.
  • the cleaning temperature is preferably 15 ° C. or higher, more preferably 25 ° C. or higher, from the viewpoint of removal of the support material, reduction of damage to the three-dimensional object, and economy, although it depends on the type of model material. More preferably, the temperature is more preferably 40 ° C. or more, more preferably 40 ° C. or more, and from the same viewpoint, 85 ° C. or less is preferable, and 70 ° C. or less is more preferable.
  • the support material of the present embodiment is a support material that supports a three-dimensional object when the three-dimensional object is manufactured by a hot melt lamination type 3D printer, and includes the polyamide resin.
  • the support material can suppress foaming and suppress deterioration in accuracy of a three-dimensional object even when used for manufacturing a three-dimensional object by a 3D printer after being exposed to high humidity.
  • the dissolution rate is high, and the support material can be quickly removed from the three-dimensional object precursor without using a strong alkaline aqueous solution.
  • the reason why the support material has such an effect is not certain, but the same reason as the reason why the soluble material for three-dimensional modeling has the effect can be considered.
  • the present specification further discloses the following composition and production method.
  • a three-dimensional modeling soluble material used as a material of a support material for supporting a three-dimensional object when a three-dimensional object is manufactured by a hot melt lamination type 3D printer,
  • the material includes a polyamide resin, and the polyamide resin has a hydrophilic monomer unit A having a hydrophilic group, a hydrophobic dicarboxylic acid monomer unit B, and a hydrophobic diamine monomer unit C, and all the monomer units in the polyamide resin
  • the three-dimensional modeling soluble material wherein the ratio of the hydrophilic monomer unit A to the total is 2.5 mol% or more and less than 13.5 mol%.
  • the hydrophilic group is a primary amino group, a secondary amino group, a tertiary amino group, a quaternary ammonium base, an oxyethylene group, a hydroxyl group, a carboxyl group, a carboxyl base, a phosphate group,
  • the soluble material for three-dimensional modeling according to ⁇ 1> comprising at least one selected from the group consisting of a phosphate group, a sulfonate group, and a sulfonate group.
  • a secondary amino group in which the secondary amino group is represented by —NHR 1 group (wherein R 1 represents a linear or branched alkyl group having 1 to 14 carbon atoms).
  • At least one selected from the group consisting of secondary amino groups represented by —NH— groups is preferably the soluble material for three-dimensional modeling according to ⁇ 2>.
  • the tertiary amino group is a —NR 2 R 3 group (wherein R 2 represents a linear or branched alkyl group having 1 to 4 carbon atoms, and R 3 represents a linear or branched group.
  • a —NR 4 — group (wherein R 4 is a linear or branched carbon group having 1 to 4 carbon atoms).
  • the quaternary ammonium base is —N + ⁇ R 5 R 6 R 7 ⁇ ⁇ X ⁇ (where R 5 , R 6 and R 7 are each independently a hydrogen atom or a carbon number of 1 or more and 14 X ⁇ represents a hydroxy ion, a halogen ion, CH 3 SO 4 — or CH 3 CH 2 SO 4 — )), and at least selected from the group consisting of quaternary ammonium bases
  • the oxyethylene group is — ⁇ CH 2 CH 2 O ⁇ n — (where n represents an average number, represents a number of 1 to 2500, preferably 2 to 1000, preferably 3 to 100 More preferably 4 or more and 50 or less), and — ⁇ CH 2 CH 2 O ⁇ m —R 8 (where m represents an average number and 1 or more and 2500 or less). It is preferably 2 or more and 1000 or less, more preferably 3 or more and 100 or less, and still more preferably 4 or more and 50 or less, and R 8 represents a hydrogen atom or a linear or branched alkyl group having 1 to 10 carbon atoms.
  • At least one selected from the group consisting of oxyethylene groups represented by the formula (2) to ⁇ 5> is preferred.
  • the carboxyl base is —COOM 1 (where M 1 represents a counter ion of the carboxyl group constituting the carboxyl base, and sodium ion, potassium ion, lithium ion, calcium from the viewpoint of solubility in neutral water)
  • At least one selected from the group consisting of ions, magnesium ions, ammonium ions, barium ions, and zinc ions is preferred, and at least one selected from the group consisting of sodium ions, potassium ions, lithium ions, magnesium ions, and ammonium ions.
  • the phosphate group is —PO 4 M 2 2 , —PO 4 HM 2 , or —PO 4 M 2 (where M 2 represents a counter ion of a phosphate group constituting the phosphate group, From the viewpoint of solubility in basic water, at least one selected from the group consisting of sodium ion, potassium ion, lithium ion, calcium ion, magnesium ion, ammonium ion, barium ion, and zinc ion is preferable.
  • Sodium ion, potassium At least one selected from the group consisting of ions, lithium ions, magnesium ions, and ammonium ions is more preferable, at least one selected from the group consisting of sodium ions and potassium ions is more preferable, and sodium ions are even more preferable. Preferably). More least one preferably selected, ⁇ 2> to ⁇ 7> 3D modeling for soluble material as claimed in any one.
  • the sulfonate group is —SO 3 M 3 (wherein M 3 represents a counter ion of a sulfonate group constituting the sulfonate group, and from the viewpoint of solubility in neutral water, sodium ion and potassium ion) And preferably at least one selected from the group consisting of lithium ions, calcium ions, magnesium ions, ammonium ions, barium ions, and zinc ions, and a group consisting of sodium ions, potassium ions, lithium ions, magnesium ions, and ammonium ions At least one selected from the group consisting of sodium ions and potassium ions is more preferable, and sodium ions are more preferable.
  • the monomer A for deriving the hydrophilic monomer unit A is preferably at least one selected from the group consisting of carboxylic acid, amine and amino acid, more preferably carboxylic acid, ⁇ 1> to ⁇ 9>
  • the carboxylic acid is preferably an aromatic carboxylic acid, a hydroxy group-containing aromatic dicarboxylic acid, a primary amino group-containing aromatic dicarboxylic acid, a sulfonic acid group-containing aromatic dicarboxylic acid, and a sulfonate group-containing aromatic.
  • dicarboxylic acids such as 5-hydroxyisophthalic acid, 1,3,5-benzenetricarboxylic acid, 5-aminoisophthalic acid, 5-sulfoisophthalic acid, 2-sulfoterephthalic acid, and 4-sulfo-2,6-naphthalene. At least one selected from the group consisting of dicarboxylic acids is more preferable, at least one selected from the group consisting of 5-sulfoisophthalic acid and 2-sulfoterephthalic acid is still more preferable, and 5-sulfoisophthalic acid is more preferable. More preferably, the soluble material for three-dimensional modeling according to ⁇ 10>.
  • the hydrophilic group content in the polyamide resin is preferably 0.5 mmol / g or more, more preferably 0.6 mmol / g or more, still more preferably 0.7 mmol / g or more, and 1.0 mmol /
  • the ratio of the substance amount of the hydrophilic monomer unit A to the total substance amount of all monomer units in the polyamide resin is 2.5 mol% or more, preferably 4 mol% or more, more preferably 6 mol% or more.
  • 8 mol% or more is more preferable
  • 10 mol% or more is more preferable, less than 13.5 mol%, 11.5 mol% or less is preferable, 10.0 mol% or less is more preferable, and 9.5 mol% or less is more preferable.
  • the dicarboxylic acid B for deriving the hydrophobic dicarboxylic acid monomer unit B is preferably at least one selected from the group consisting of aromatic dicarboxylic acids, aliphatic dicarboxylic acids, and alicyclic dicarboxylic acids, At least one selected from the group consisting of terephthalic acid, isophthalic acid, 2,5-furandicarboxylic acid, 2,6-naphthalenedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, and 1,3-adamantanedicarboxylic acid is more Preferably, at least one selected from the group consisting of terephthalic acid, 2,5-furandicarboxylic acid, and 2,6-naphthalenedicarboxylic acid is more preferable, and terephthalic acid is still more preferable.
  • the soluble material for three-dimensional modeling described in Crab. ⁇ 15> The ratio of the substance amount of the hydrophobic dicarboxylic acid monomer unit B in the polyamide resin to the total substance amount of all monomer units in the polyamide resin is preferably 10 mol% or more, more preferably 20 mol% or more. 30 mol% or more, more preferably 35 mol% or more, still more preferably 40 mol% or more, still more preferably 42 mol% or more, further preferably 47.5 mol% or less, more preferably 45 mol% or less, and 42 mol% or less.
  • the molar ratio of the hydrophilic monomer unit A to the hydrophobic dicarboxylic acid monomer unit B is preferably 10/90 or more, and 15/85
  • the above is more preferable, 18/82 or more is further preferable, 20/80 or more is more preferable, less than 27/73 is preferable, 25/75 or less is more preferable, and 21/79 or less is more preferable, ⁇ 1> to ⁇ 15>
  • the soluble material for three-dimensional modeling according to any one of the above.
  • the diamine C for deriving the hydrophobic diamine monomer unit C is preferably at least one selected from the group consisting of an aliphatic diamine, an alicyclic diamine, and an aromatic diamine, and more preferably an aliphatic diamine.
  • the carbon number of the diamine C for deriving the hydrophobic diamine monomer unit C is preferably 2 or more, more preferably 3 or more, still more preferably 4 or more, preferably 20 or less, more preferably 15 or less, The soluble material for three-dimensional modeling according to any one of ⁇ 1> to ⁇ 17>, further preferably 10 or less.
  • the aliphatic diamine is at least one selected from the group consisting of ethylenediamine, trimethylenediamine, tetramethylenediamine, pentamethylenediamine, hexamethylenediamine, heptamethylenediamine, octamethylenediamine, nonanediamine, and decanediamine.
  • the alicyclic diamine is preferably at least one selected from the group consisting of 4,4′-diamino-3,3′-dimethyldicyclohexylmethane, diaminecyclohexane and isophoronediamine, and diaminecyclohexane and isophorone.
  • the aromatic diamine is preferably at least one selected from the group consisting of phenylenediamine, diethyltoluenediamine, and 4,4′-diaminodiphenylmethane, and at least selected from the group consisting of phenylenediamine and diethyltoluenediamine.
  • the diamine C for deriving the hydrophobic diamine monomer unit C is preferably at least one selected from the group consisting of hexamethylene diamine, diamine cyclohexane and phenylene diamine, and a group consisting of hexamethylene diamine and phenylene diamine.
  • the diamine C for deriving the hydrophobic diamine monomer unit C is at least one selected from the group consisting of hexamethylene diamine, diamine cyclohexane and phenylene diamine, all diamine monomer units in the polyamide resin
  • the ratio of the total amount of hexamethylenediamine, diaminecyclohexane, and phenylenediamine to the total amount of these is preferably 50 mol% or more, more preferably 70 mol% or more, still more preferably 80 mol% or more, and more preferably 90 mol% or more.
  • the soluble material for three-dimensional modeling according to any one of ⁇ 1> to ⁇ 22> which is substantially more preferably 100 mol%, still more preferably 100 mol%.
  • p1 and q1 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water.
  • p2 and q2 each represent the number of polymerization degrees.
  • Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water.
  • p3 and q3 each represent the number of polymerization degrees.
  • Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water.
  • p4 and q4 each represent the number of polymerization degrees.
  • Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water.
  • p5 and q5 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water.
  • p6 and q6 each represent the number of polymerization degrees. Each polymerization is a block bond and / or a random bond, and a random bond is more preferable from the viewpoint of solubility in neutral water.
  • the weight average molecular weight of the polyamide resin is preferably 3000 or more, more preferably 3500 or more, further preferably 4000 or more, preferably 70000 or less, more preferably 50000 or less, still more preferably 30000 or less, and more preferably 20000 or less. More preferably, the soluble material for three-dimensional modeling according to any one of ⁇ 1> to ⁇ 24>.
  • the glass transition temperature of the polyamide resin is preferably 50 ° C. or higher, more preferably 60 ° C. or higher, still more preferably 70 ° C. or higher, still more preferably 80 ° C. or higher, preferably 250 ° C. or lower, and 220 ° C. or lower.
  • the content of the polyamide resin in the three-dimensional modeling soluble material is preferably 30% by mass or more, more preferably 50% by mass or more, still more preferably 60% by mass or more, and even more preferably 70% by mass or more.
  • 80% by mass or more is more preferable, 90% by mass or more is further preferable, 95% by mass or more is further preferable, substantially 100% by mass is further more preferable, and 100% by mass is further more preferable, ⁇ 1
  • the glass transition temperature of the three-dimensional modeling soluble material is preferably 50 ° C or higher, more preferably 60 ° C or higher, still more preferably 70 ° C or higher, still more preferably 80 ° C or higher, and preferably 250 ° C or lower,
  • the shape of the three-dimensional modeling soluble material is preferably at least one selected from the group consisting of pellets, powders, and filaments, more preferably filaments, ⁇ 1> to ⁇ 28> The soluble material for 3D modeling described.
  • the shape of the three-dimensional modeling soluble material is a filament
  • the filament has a diameter of preferably 0.5 mm or more, more preferably 1.0 mm or more, preferably 3.0 mm or less, 2.0 mm
  • a hot melt lamination method having a step of obtaining a three-dimensional object precursor including a three-dimensional object and a support material, and a support material removing step of bringing the three-dimensional object precursor into contact with neutral water and removing the support material
  • a modeling material which is a material of a three-dimensional object is ABS resin, polylactic acid resin, polycarbonate resin, 12-nylon, 6,6-nylon, 6-nylon, polyphenylsulfone resin, polyetheretherketone, and The method for producing a three-dimensional object according to ⁇ 31>, wherein at least one selected from the group consisting of polyetherimide is preferable, ABS resin and / or polylactic acid resin is more preferable, and ABS resin is more preferable.
  • the water-soluble organic solvent is a lower alcohol such as methanol, ethanol, 2-propanol, glycol ethers such as propylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monotertiary butyl ether, diethylene glycol monobutyl ether,
  • the content of the water-soluble organic solvent in the neutral water is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, further preferably 1% by mass or more, and further preferably 3% by mass or more.
  • the amount of the neutral water used is preferably 10 times by mass or more, more preferably 20 times by mass or more, more preferably 10,000 times by mass or less, and preferably 5000 times by mass or less with respect to the support material.
  • the hydrophilic monomer unit A, the hydrophobic dicarboxylic acid monomer unit B, and the hydrophobic diamine monomer unit C are included, and the ratio of the hydrophilic monomer unit A to the total of all monomer units in the polyamide resin is 2.
  • the support material which is 5 mol% or more and less than 13.5 mol%.
  • the polyamide resin is a polyamide resin used for the three-dimensional modeling soluble material according to any one of ⁇ 1> to ⁇ 30>.
  • the hydrophilic monomer amount (mmol / g) in the polyamide was calculated from the composition of the hydrophilic monomer unit determined by the analysis method according to the following formula. However, the number of moles of all dicarboxylic acid monomer units and the number of moles of all amine monomer units were assumed to be equal.
  • Mc molecular weight of hydrophobic dicarboxylic acid other than hydrophilic monomer (however, when there are a plurality of dicarboxylic acid species, number average molecular weight)
  • the amount (unit: mmol / g) of hydrophilic groups in the polyamide resin was determined from the composition of the polyamide resin determined by the above method.
  • Measurement device HLC-8320GPC (manufactured by TOSOH) Eluent: HFIP / 0.5 mM sodium trifluoroacetate Flow rate: 0.2 mL / min ⁇ Measurement temperature: 40 °C ⁇
  • Glass transition temperature of polyamide resin A sample of 5 to 10 mg is precisely weighed and sealed in an aluminum pan, and the temperature is increased from 30 ° C. to 350 ° C. at 10 ° C./min using a differential scanning calorimeter “DSC device (DSC7020 manufactured by Seiko Instruments Inc.). And then rapidly cooled to 30 ° C. From the DSC curve obtained by raising the temperature again to 350 ° C. at 10 ° C./min, the glass transition temperature (° C.), melting point (° C.), crystallization temperature (° C.) Asked.
  • DSC device DSC7020 manufactured by Seiko Instruments Inc.
  • the dicarboxylic acid composition, the diol composition, the amount of sulfonate group, the weight average molecular weight (Mw), the glass transition temperature (° C.), the melting point (° C.), the crystallization temperature (° C.) was determined by the analysis method.
  • the measurement results are shown in Table 1.
  • SIP (mol%) is the ratio (mol%) of 5-sulfoisophthalic acid monomer units in all dicarboxylic acid monomer units
  • TPA (mol%) is terephthalic acid monomer units in all dicarboxylic acid monomer units.
  • Ratio (mol%), IPA (mol%) is the ratio (mol%) of isophthalic acid monomer units in all dicarboxylic acid monomer units, and HMDA (mol%) is the ratio of hexamethylenediamine monomer units in all diamine monomer units.
  • Mol%) and the amount of sulfonic acid group (mmol / g) indicate the amount of sulfonic acid group (mmol / g) in the polyamide.
  • Tg means glass transition temperature and Tc means crystallization temperature.
  • Example 1 to 3 and Comparative Examples 1 to 5 With respect to the polyamide compounds 1 to 5 obtained in the synthesis examples described above and the following commercially available support materials 1 to 3, the solubility in neutral water and the hygroscopicity were evaluated by the analysis method. The analysis results are shown in Table 1.
  • the commercial products 1 to 3 in Table 1 are as follows.

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Abstract

L'invention concerne un matériau fusible destiné à un moulage tridimensionnel, utilisé comme matériau support pour supporter un objet tridimensionnel lors de la fabrication de l'objet tridimensionnel à l'aide d'une imprimante 3D à dépôt de fil fondu (fused deposition modeling - FDM). Le matériau fusible destiné à un moulage tridimensionnel contient une résine de polyamide présentant : un motif monomère hydrophile A présentant un groupe hydrophile ; un motif monomère de type acide dicarboxylique hydrophobe B ; et un motif monomère de type diamine hydrophobe C, la proportion du motif monomère hydrophile A par rapport à la somme de tous les motifs monomères dans la résine de polyamide étant d'au moins 2,5 % en mole et inférieure à 13,5 % en mole. Ce matériau fusible destiné à un moulage tridimensionnel est utilisé comme matériau support et convient pour la fabrication d'un objet tridimensionnel par le procédé FDM, présente une résistance à l'absorption d'humidité, présente une vitesse de dissolution élevée dans l'eau neutre et peut être rapidement éliminé d'un précurseur d'objet tridimensionnel sans utiliser de solution aqueuse fortement alcaline.
PCT/JP2017/026700 2016-07-28 2017-07-24 Matériau fusible destiné à un moulage tridimensionnel WO2018021243A1 (fr)

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US16/320,940 US20190160732A1 (en) 2016-07-28 2017-07-24 Fusible material for three-dimensional molding
CN201780046726.0A CN109476840B (zh) 2016-07-28 2017-07-24 三维造型用可溶性材料
EP17834249.9A EP3492511A4 (fr) 2016-07-28 2017-07-24 Matériau fusible destiné à un moulage tridimensionnel

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3495108A4 (fr) * 2016-08-05 2020-03-11 Kao Corporation Procédé de production d'un matériau fusible destiné à un moulage tridimensionnel

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5092996A (fr) * 1973-12-22 1975-07-24
JPS57167339A (en) * 1981-04-08 1982-10-15 Unitika Ltd Preparation of resin composition with excellent water resistance
JPH05210241A (ja) * 1992-01-30 1993-08-20 Toray Ind Inc 感光性樹脂印刷版
JPH07258407A (ja) * 1994-03-23 1995-10-09 Tomoegawa Paper Co Ltd スルホン酸基含有ポリアミドの製造方法
JP2007231087A (ja) * 2006-02-28 2007-09-13 Toray Ind Inc 水溶性ポリアミド水溶液の製造法
JP2010159414A (ja) * 2008-12-12 2010-07-22 Emg-Patent Ag ポリアミド層状シリケート組成物
JP2011518938A (ja) * 2008-04-29 2011-06-30 アルケマ フランス ポリアミド粉末の溶融温度と結晶化温度との差を広げる方法
JP2015519456A (ja) * 2012-06-12 2015-07-09 ロディア オペレーションズRhodia Operations 粉末の熱処理方法
JP2016501136A (ja) * 2012-11-09 2016-01-18 エボニック インダストリーズ アクチエンゲゼルシャフトEvonik Industries AG 多色の押出し成形3d印刷
JP2016078284A (ja) * 2014-10-14 2016-05-16 花王株式会社 三次元造形用可溶性材料
WO2016125860A1 (fr) * 2015-02-06 2016-08-11 花王株式会社 Matériau soluble de modélisation tridimensionnelle

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5092996A (fr) * 1973-12-22 1975-07-24
JPS57167339A (en) * 1981-04-08 1982-10-15 Unitika Ltd Preparation of resin composition with excellent water resistance
JPH05210241A (ja) * 1992-01-30 1993-08-20 Toray Ind Inc 感光性樹脂印刷版
JPH07258407A (ja) * 1994-03-23 1995-10-09 Tomoegawa Paper Co Ltd スルホン酸基含有ポリアミドの製造方法
JP2007231087A (ja) * 2006-02-28 2007-09-13 Toray Ind Inc 水溶性ポリアミド水溶液の製造法
JP2011518938A (ja) * 2008-04-29 2011-06-30 アルケマ フランス ポリアミド粉末の溶融温度と結晶化温度との差を広げる方法
JP2010159414A (ja) * 2008-12-12 2010-07-22 Emg-Patent Ag ポリアミド層状シリケート組成物
JP2015519456A (ja) * 2012-06-12 2015-07-09 ロディア オペレーションズRhodia Operations 粉末の熱処理方法
JP2016501136A (ja) * 2012-11-09 2016-01-18 エボニック インダストリーズ アクチエンゲゼルシャフトEvonik Industries AG 多色の押出し成形3d印刷
JP2016078284A (ja) * 2014-10-14 2016-05-16 花王株式会社 三次元造形用可溶性材料
WO2016125860A1 (fr) * 2015-02-06 2016-08-11 花王株式会社 Matériau soluble de modélisation tridimensionnelle

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3495108A4 (fr) * 2016-08-05 2020-03-11 Kao Corporation Procédé de production d'un matériau fusible destiné à un moulage tridimensionnel

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